IP Library Granted Patent US 10,245,331
Granted Patent B2
US 10,245,331 · App. 15/899,644 · Granted Apr 2, 2019

Cromolyn derivatives and related methods of imaging and treatment

Inventor: David R. Elmaleh (Newton, MA)
Assignee: The General Hospital Corporation
A61K51/0421C07D311/24
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Quick Facts
Patent No.
US 10,245,331
App. No.
15/899,644
Granted
Apr 2, 2019
Kind
B2
Abstract

Novel cromolyn analogs useful as imaging agents for detecting atherosclerotic plaques and for treating atherosclerosis and Alzheimer's Disease, and methods of making the cromolyn analogs, are disclosed. The cromolyn analogs have the general formula: wherein: X is OH, C 1 -C 6 alkoxyl; Y and Z are independently selected form a C 1 -C 6 alkyl, C 1 -C 6 alkoxyl, halogen, un-substituted or C 1 -C 6 substituted amine, 18 F, 19 F, or H; and n is 1, 2, or 3; and wherein for structure (I), if n are both 1 and Y and Z are both H and X is OH.

Claims (17)

1. A method for treating Alzheimer's disease in a subject in need thereof consisting of co-administering:

by inhalation cromolyn sodium in the form of a dry powder, and

by mouth from 1 mg to 25 mg of ibuprofen per day,

wherein the dry powder is micronized and further comprises an excipient.

2. The method of claim 1 , wherein 1 mg, 2 mg, 5 mg, 10 mg, or 25 mg of ibuprofen per day are co-administered.

3. The method of claim 1 , wherein 1 mg, 2 mg, 5 mg, or 10 mg of ibuprofen per day are co-administered.

4. The method of claim 1 , wherein 10 mg or 25 mg of ibuprofen per day are co-administered.

5. The method of claim 1 , wherein the excipient is lactose monohydrate.

6. The method of claim 1 , wherein 0.05 to 0.5 mg/kg per day of cromolyn sodium are administered.

7. The method of claim 1 , wherein the dry powder further comprises a pharmaceutically acceptable carrier.

8. A method for treating Alzheimer's disease in a subject in need thereof consisting of co-administering:

by inhalation cromolyn sodium in the form of a dry powder, and

by mouth 10 mg of ibuprofen per day,

wherein the dry powder is micronized and further comprises an excipient.

9. The method of claim 8 , wherein the excipient is lactose monohydrate.

10. The method of claim 8 , wherein 0.05 to 0.5 mg/kg per day of cromolyn sodium are administered.

11. The method of claim 8 , wherein the dry powder further comprises a pharmaceutically acceptable carrier.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 15, 2018
From: ELMALEH, DAVID R.
To: THE GENERAL HOSPITAL CORPORATION
Reel/Frame 045808/0554 →
Continuity (4)
Continuation 14059924 · Oct 22, 2013
Continuation In Part 13146842
Provisional Application 61148245 · Jan 29, 2009
Related Publication 20180169277A1 · Jun 21, 2018
Cited By (4)
US 12,383,528 US 12,458,622 US 12,605,471 US 12,612,391